Cardanol monoene

Base Information

• Chemical Name: Cardanol monoene
• CAS No.: 501-26-8
• Deprecated CAS: 29322-12-1
• Molecular Formula: C21H34O
• Molecular Weight: 302.5
• Hs Code.: 2907199090
• UNII: V7D0J5LYPB
• ChEMBL ID: CHEMBL470263
• DSSTox Substance ID: DTXSID30872878
• Metabolomics Workbench ID: 70457
• Nikkaji Number: J167.345I
• Wikidata: Q27105256
• Mol file: 501-26-8.mol

Synonyms:Cardanol monoene;501-26-8;Cardanol (C15:1);Ginkgol;3-[(Z)-pentadec-8-enyl]phenol;(15:1)-Cardanol;(Z)-3-(pentadec-8-en-1-yl)phenol;5-{8(Z)-Pentadecenyl}Phenol;V7D0J5LYPB;Phenol, 3-(8-pentadecenyl)-, (Z)-;CHEBI:146;CHEMBL470263;m-[(Z)-8-Pentadecenyl]phenol;(Z)-3-(8-Pentadecenyl)phenol;Phenol, 3-(8Z)-8-pentadecenyl-;3-[8(z)-pentadecenyl]phenol;3-(8(Z)-pentadecenyl)phenol;Cardanol C15:1;AC1NQZ6O;UNII-V7D0J5LYPB;SureCN2291238;SCHEMBL2291238;3-[(Z)-8-Pentadecenyl]phenol;DTXSID30872878;(Z)-3-(pentadec-8-enyl)phenol;3-[8''(Z)-pentadecenyl]phenol;YLKVIMNNMLKUGJ-FPLPWBNLSA-N;PHENOL, M-8-PENTADECENYL-,;Phenol, m-8-pentadecenyl-, (Z)-;BDBM50242263;LMPK15010007;AKOS040761464;FS-8027;3-[(8Z)-Pentadec-8-en-1-yl]phenol;Phenol, 3-(8Z)-8-pentadecen-1-yl-;HY-119979;CS-0078860;(Z)- 3-(8Z)-8-PENTADECEN-1-YLPHENOL;Q27105256

Chemical Property of Cardanol monoene

Chemical Property:

• Vapor Pressure: 3.45E-08mmHg at 25°C
• Boiling Point: 435.4°Cat760mmHg
• PKA: 10.06±0.10(Predicted)
• Flash Point: 196.6°C
• PSA: 20.23000
• Density: 0.919g/cm³
• LogP: 6.80190
• XLogP3: 8.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 13
• Exact Mass: 302.260965704
• Heavy Atom Count: 22
• Complexity: 259

Purity/Quality:

98%min ^*data from raw suppliers

Cardanol monoene ≥98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCC=CCCCCCCCC1=CC(=CC=C1)O
• Isomeric SMILES: CCCCCC/C=C\CCCCCCCC1=CC(=CC=C1)O

Technology Process of Cardanol monoene

There total 4 articles about Cardanol monoene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3-<(Z)-pentadec-8-enyl>anisole (40586-09-2) → 3-[(Z)-8-pentadecenyl]phenol (501-26-8)

Guidance literature:

With boron tribromide; In dichloromethane; at -70 ℃; for 3h;

Reference yield:

3-(pentadec-8-ynyl)phenol → 3-[(Z)-8-pentadecenyl]phenol (501-26-8)

Guidance literature:

With quinoline; hydrogen; palladium on barium sulfate; In methanol; Ambient temperature;

Reference yield:

(15:1)-Δ8-anacardic acid (76261-14-8) → 3-[(Z)-8-pentadecenyl]phenol (501-26-8)

Guidance literature:

at 240 ℃;

upstream raw materials:

3-<(Z)-pentadec-8-enyl>anisole

(15:1)-Δ⁸-anacardic acid

Downstream raw materials:

O-acetyl 3-(8'(Z)-pentadecenyl)phenol

3-Pentadecylphenoxyacetic acid

3-n-Pentadecylphenol

3-pentadecylcyclohexanol

Refernces